Crossey PA - Search Results

1

Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas.

Eng C, Crossey PA, Mulligan LM, Healey CS, Houghton C, Prowse A, Chew SL, Dahia PL, O'Riordan JL, Toledo SP, et al. Eng C, et al. Among authors: crossey pa. J Med Genet. 1995 Dec;32(12):934-7. doi: 10.1136/jmg.32.12.934. J Med Genet. 1995. PMID: 8825918 Free PMC article.

2

Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytoma.

Crossey PA, Eng C, Ginalska-Malinowska M, Lennard TW, Wheeler DC, Ponder BA, Maher ER. Crossey PA, et al. J Med Genet. 1995 Nov;32(11):885-6. doi: 10.1136/jmg.32.11.885. J Med Genet. 1995. PMID: 8592333 Free PMC article.

3

Somatic mutations of the von Hippel-Lindau disease tumour suppressor gene in non-familial clear cell renal carcinoma.

Foster K, Prowse A, van den Berg A, Fleming S, Hulsbeek MM, Crossey PA, Richards FM, Cairns P, Affara NA, Ferguson-Smith MA, et al. Foster K, et al. Among authors: crossey pa. Hum Mol Genet. 1994 Dec;3(12):2169-73. doi: 10.1093/hmg/3.12.2169. Hum Mol Genet. 1994. PMID: 7881415

4

Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype.

Crossey PA, Richards FM, Foster K, Green JS, Prowse A, Latif F, Lerman MI, Zbar B, Affara NA, Ferguson-Smith MA, et al. Crossey PA, et al. Hum Mol Genet. 1994 Aug;3(8):1303-8. doi: 10.1093/hmg/3.8.1303. Hum Mol Genet. 1994. PMID: 7987306

5

Detailed genetic mapping of the von Hippel-Lindau disease tumour suppressor gene.

Richards FM, Maher ER, Latif F, Phipps ME, Tory K, Lush M, Crossey PA, Oostra B, Enblad P, Gustavson KH, et al. Richards FM, et al. Among authors: crossey pa. J Med Genet. 1993 Feb;30(2):104-7. doi: 10.1136/jmg.30.2.104. J Med Genet. 1993. PMID: 8445612 Free PMC article.

6

Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations.

Maher ER, Webster AR, Richards FM, Green JS, Crossey PA, Payne SJ, Moore AT. Maher ER, et al. Among authors: crossey pa. J Med Genet. 1996 Apr;33(4):328-32. doi: 10.1136/jmg.33.4.328. J Med Genet. 1996. PMID: 8730290 Free PMC article.

7

Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type II.

Neumann HP, Eng C, Mulligan LM, Glavac D, Zäuner I, Ponder BA, Crossey PA, Maher ER, Brauch H. Neumann HP, et al. Among authors: crossey pa. JAMA. 1995 Oct 11;274(14):1149-51. JAMA. 1995. PMID: 7563486

8

Isolated familial pheochromocytoma as a variant of von Hippel-Lindau disease.

Ritter MM, Frilling A, Crossey PA, Höppner W, Maher ER, Mulligan L, Ponder BA, Engelhardt D. Ritter MM, et al. Among authors: crossey pa. J Clin Endocrinol Metab. 1996 Mar;81(3):1035-7. doi: 10.1210/jcem.81.3.8772572. J Clin Endocrinol Metab. 1996. PMID: 8772572

9

Detailed mapping of germline deletions of the von Hippel-Lindau disease tumour suppressor gene.

Richards FM, Crossey PA, Phipps ME, Foster K, Latif F, Evans G, Sampson J, Lerman MI, Zbar B, Affara NA, et al. Richards FM, et al. Among authors: crossey pa. Hum Mol Genet. 1994 Apr;3(4):595-8. doi: 10.1093/hmg/3.4.595. Hum Mol Genet. 1994. PMID: 8069305

10

Mapping the Von Hippel-Lindau disease tumour suppressor gene: identification of germline deletions by pulsed field gel electrophoresis.

Richards FM, Phipps ME, Latif F, Yao M, Crossey PA, Foster K, Linehan WM, Affara NA, Lerman MI, Zbar B, et al. Richards FM, et al. Among authors: crossey pa. Hum Mol Genet. 1993 Jul;2(7):879-82. doi: 10.1093/hmg/2.7.879. Hum Mol Genet. 1993. PMID: 8364570

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